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Patient Recruitment Specialist – Pennsylvania (Full-time)

Pennsylvania

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Full-time

Job Summary

The Patient Recruitment Specialist works independently to help recruit and pre-screen potential study volunteers across sites for protocol eligibility. This is a remote position, however may require to visit the SRA site in PA on occasion.

Work Schedule

Work schedule includes weekend hours:

Tuesday through Saturday OR Wednesday – Sunday 9:30 am to 6:00 pm EST

Key Responsibilities

Be familiar with the purpose, inclusion and exclusion criteria, telephone screening scripts, goals/timelines and scheduling for all enrolling trials
Telephone pre-screen inbound and outbound volunteers for clinical trial participation
Pre-identify appropriate volunteers by using the clinical trial management system to review volunteer’s documented medical history, current medications, and study history to assess potential eligibility
Conduct telephone screening questionnaire to see if potential volunteers qualify
Use clinical trial management system and study specific telephone screening scripts to:
Review and update volunteer information
Take a careful history, reviewing volunteer’s pertinent medical history
Review volunteer’s current medications to determine if they are exclusionary
Assess volunteer’s interest and willingness to commit to the course of the trial
Determine appropriateness of volunteer
Schedule and reschedule appointments as directed
Escalate clinical questions to Recruitment Manager as needed
Learn the medication categories that may be excluded in each protocol
Stay abreast of protocol amendments and how they affect screening
Obtain medical records as required per protocol
Ability to meet metrics requirements that are set by senior management
Work with supervisor to achieve recruitment goals and deadlines for each study.
Perform other specialized duties as assigned by the manager

Qualifications

High school diploma or GED, some college preferred
Prefer candidates who reside in the state of Pennsylvania
Interest or background in Psychology a plus!
Medical background, familiarity with medical terminology or trial experience knowledge preferred
Excellent people and phone communication skills. Solid organizational skills including attention to detail, critical thinking and multi-tasking skills.
Ability to work cooperatively and effectively within the team and the organization
Ability to learn clinical trial management software.
Ability to adapt quickly to changing work demand

Wage:  $20-22/hour

EOE Statement Atlas Clinical Research and its affiliates are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law. Apply Now

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Candidate Information

Max. file size: 56 MB.
Accepted file types: pdf.
Max. file size: 56 MB.
Accepted file types: pdf.

Work Authorization

Are you legally authorized to work in the United States?**
Will you now or in the future require a visa sponsorship?**

References

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